U.S. patent number 4,224,309 [Application Number 06/069,464] was granted by the patent office on 1980-09-23 for antibacterial oral composition.
This patent grant is currently assigned to Colgate-Palmolive Company. Invention is credited to Abdul Gaffar, John J. Grecsek.
United States Patent |
4,224,309 |
Gaffar , et al. |
September 23, 1980 |
Antibacterial oral composition
Abstract
An antibacterial oral composition effective to promote oral
hygiene containing an antibacterial antiplaque agent which normally
stains dental surfaces and an additive which reduces such staining
without substantially diminishing the antibacterial and antiplaque
activity of the agent. Bis-biguanido hexanes, such as
chlorohexidine and alexidine, and quaternary ammonium salts, such
as benzethonium chloride and cetyl pyridinium chloride are typical
examples of antibacterial agents. The antistain additive is
2-phosphono-butane-1,2,4-tricarboxylic acid compound or an orally
acceptable salt thereof.
Inventors: |
Gaffar; Abdul (Somerset,
NJ), Grecsek; John J. (Trenton, NJ) |
Assignee: |
Colgate-Palmolive Company (New
York, NY)
|
Family
ID: |
22089135 |
Appl.
No.: |
06/069,464 |
Filed: |
August 24, 1979 |
Current U.S.
Class: |
424/54;
424/49 |
Current CPC
Class: |
A61K
8/55 (20130101); A61Q 11/00 (20130101); A61K
2800/52 (20130101) |
Current International
Class: |
A61K
8/55 (20060101); A61K 8/30 (20060101); A61Q
11/00 (20060101); A61K 007/22 (); A61K
007/16 () |
Field of
Search: |
;424/49-58 |
References Cited
[Referenced By]
U.S. Patent Documents
Primary Examiner: Rose; Shep K.
Attorney, Agent or Firm: Sylvester; Herbert S. Grill; Murray
M. Blumenkopf; Norman
Claims
What is claimed is:
1. An oral composition comprising an oral vehicle, at least one
nitrogen-containing antibacterial antiplaque agent, whose use has
been observed to lead to staining or discoloration of dental
surfaces, selected from the group consisting of cationic
antibacterial antiplaque agent and long chain amine antibacterial
antiplaque agent containing a fatty alkyl group of about 12 to 18
carbon atoms and as anti-staining additive, an effective
stain-inhibiting amount of a
2,-phosphono-butane-1,2,4-tricarboxylic acid compound of the
formula ##STR5## wherein R is hydrogen, lower alkyl or carboxyl,
and R.sup.1 is hydrogen or methyl, or an orally acceptable salt
thereof.
2. The oral composition of claim 1 wherein R and R.sup.1 are
hydrogen.
3. The oral composition of claims 1 or 2 wherein said antibacterial
antiplaque agent is present in an amount of about 0.001 to about
15% by weight based on the free base form of said agent and said
additive is present in an amount of about 0.01 to about 10% by
weight.
4. The oral composition of claims 1 or 2 wherein said antibacterial
antiplaque agent is present in an amount of about 0.01 to about 5%
by weight, based on its free base form.
5. The oral composition of claims 1 or 2 wherein said antibacterial
antiplaque agent is a substituted guanidine.
6. The oral composition of claims 1 or 2 wherein said antibacterial
antiplaque agent is a pharmaceutically acceptable water soluble
salt of an agent selected from the group consisting of
chlorhexidine and alexidine.
7. The oral composition of claims 1 or 2 wherein said antibacterial
antiplaque agent is a pharmaceutically acceptable water soluble
salt of chlorhexidine.
8. The oral composition of claims 1 or 2 wherein said antibacterial
antiplaque agent is benzethonium chloride.
9. The oral composition of claims 1 or 2 wherein said antibacterial
antiplaque agent is a quaternary ammonium compound containing 1 to
2 alkyl groups of 8 to 20 carbon atoms.
10. The oral composition of claims 1 or 2 wherein said
antibacterial antiplaque agent is cetyl pyridinium chloride.
11. The oral composition of claims 1 or 2 wherein said vehicle is
an aqueous-alcohol and said composition is a mouthwash of pH of
about 4.5 to about 9.
12. The oral composition of claims 1 or 2 wherein said vehicle
comprises a liquid vehicle and a gelling agent and a dentally
acceptable polishing material is present and said composition is a
toothpase of pH of about 4.5 to about 9.
13. The mouthwash composition of claim 11 containing about 0.01 to
about 5.0% by weight, based on its free base form, of benzethonium
chloride.
14. The mouthwash composition of claim 11 containing about 0.01 to
about 5% by weight, based on its free base form, of a water-soluble
pharmaceutically acceptable salt of chlorhexidine.
15. The mouthwash composition of claim 11 containing about 0.01 to
about 5% by weight of cetyl pyridinium chloride.
16. A method of improving oral hygiene comprising applying to the
oral cavity an effective amount of an oral composition as defined
in claims 1 or 2.
Description
This invention relates to an antibacterial oral composition which
promotes oral hygiene.
Cationic nitrogen-containing antibacterial materials are well known
in the art. See, for instance the section on "Quaternary Ammonium
and Related Compounds" in the article on "Antiseptics and
Disinfectants" in Kirk-Othmer Encyclopedia of Chemical Technology,
second edition (Vol. 2, p. 632-635), incorporated herein by
reference. Cationic materials which possess antibacterial activity
(i.e. are germicides) are used against bacteria and have been used
in oral compositions to counter plaque formation caused by bacteria
in the oral cavity.
Among the most common of these antibacterial anti-plaque quaternary
ammonium compounds is benzethonium chloride, also known as Hyamine
1622 or diisobutylphenoxyethoxyethyl dimethyl benzyl ammonium
chloride. In an oral preparation this material is highly effective
in promoting oral hygiene by reducing formation of dental plaque
and calculus, which is generally accompanied by a reduction in
caries formation and periodontal diseases. Other cationic
antibacterial agents of this type are those mentioned, for
instance, in U.S. Pat. Nos. 2,984,639, 3,325,402, 3,431,208 and
3,703,583 and British Pat. No. 1,319,396.
Other antibacterial antiplaque quaternary ammonium compounds
include those in which one or two of the substituents on the
quaternary nitrogen has a carbon chain length (typically alkyl
group) of some 8 to 20, typically 10 to 18, carbon atoms while the
remaining substituents have a lower number of carbon atoms
(typically alkyl or benzyl group), such as 1 to 7 carbon atoms,
typically methyl or ethyl groups. Dodecyl trimethyl ammonium
bromide, dodecyl dimethyl (2-phenoxyethyl) ammonium bromide, benzyl
dimethyl stearyl ammonium chloride, cetyl pyridinium chloride and
quaternized 5-amino-1,3-bis (2-ethyl-hexyl)-5-methyl hexa
hydropyrimidine are exemplary of other typical quaternary ammonium
antibacterial agents.
Other types of cationic antibacterial agents which are desirably
incorporated in oral compositions to promote oral hygiene by
reducing plaque formation are the amidines such as the substituted
guanidines e.g. chlorhexidine and the corresponding compound,
alexidine, having 2-ethylhexyl groups instead of chlorophenyl
groups and other bis-biguanides such as those described in German
patent application No. P 2,332,383 published Jan. 10, 1974, which
sets forth the following formula: ##STR1## in which A and A'
signify as the case may be either (1) a phenyl radical, which as
substituent can contain up to 2 alkyl or alkoxy groups with 1 up to
about 4C-atoms, a nitro group or a halogen atom, (2) an alkyl group
which contains 1 to about 12C-atoms, or (3) alicyclic groups with 4
to about 12C-atoms, X and X' as the case may be may represent an
alkylene radical with 1-3C atoms, z and z' are as the case may be
either zero or 1, R and R' as the case may be may represent either
hydrogen, an alkyl radical with 1 to about 12C-atoms or an aralkyl
radical with 7 to about 12C-atoms, n is a whole number of 2 to
inclusively 12 and the polymethylene chain (CH.sub.2) can be
interrupted by up to 5 ether, thioether, phenyl- or naphthyl
groups; these are available as pharmaceutically suitable salts.
Additional substituted guanidines are: N'-(4-chlorobenzyl)-N.sup.5
-(2,4-dichlorobenzyl) biguanide; p-chlorobenzyl biguanide,
4-chlorobenzhydryl guanylurea; N-3-lauroxypropyl-N.sup.5
-p-chlorobenzyl biguanide; 5,6-dichloro-2-guanidobenzimidazole; and
N-p-chlorophenyl-N.sup.5 -laurylbiguanide.
The long chain tertiary amines also possess antibacterial and
antiplaque activity. Such antibacterial agents include tertiary
amines having one fatty alkyl group (typically 12 to 18 carbon
atoms) and 2 poly(oxyethylene) groups attached to the nitrogen
(typically containing a total of from 2 to 50 ethenoxy groups per
molecule) and salts thereof with acids and compounds of the
structure: ##STR2## where R is a fatty alkyl group containing 12 to
18 carbon atoms and x, y and z total 3 or higher, as well as salts
therof. Generally, cationic agents are preferred for their
antiplaque effectiveness.
The antibacterial antiplaque compound is preferably one which has
an antibacterial activity such that its phenol co-efficient is well
over 50, more preferably well above 100, such as above about 200 or
more for S, aureus; for instance the phenol coefficient (A.O.A.C.)
of benzethonium chloride is given by the manufacturer as 410, for
S. aureus. The cationic antibacterial agent will generally be a
monomeric (or possibly dimeric) material molecular weight well
below 2,000, such as less than about 1,000. It is, however, within
the broader scope of the invention to employ a polymeric cationic
antibacterial agent. The cationic antibacterial is preferably
supplied in the form of an orally acceptable salt thereof, such as
the chloride, bromide, sulfate, alkyl sulfonate such as methyl
sulfonate and ethyl sulfonate, phenylsulfonate, such as
p-methylphenyl sulfonate, nitrate, acetate, gluconate, etc.
The nitrogen-containing cationic antibacterial agents and long
chain tertiary amine antibacterial agents effectively promote oral
hygiene, particularly by removing plaque. However, their use has
been observed to lead to staining of dental surfaces or
discoloration.
The reason for the formation of such dental stain has not been
clearly established. However, human dental enamel contains a high
proportion (about 95%) of hydroxyapatite (HAP) which includes
Ca.sup.+2 and PO.sub.4.sup.-3 ions. In the absence of dental plaque
additional Ca.sup.+2 and PO.sub.4.sup.-3, particularly from saliva,
can be deposited on the enamel and such deposits can include color
bodies which ultimately stain the tooth enamel as a calcified
deposit thereon. It can be that as the cationic or long chain
tertiary amine antibacterial agents remove plaque they also
denature protein from saliva in the oral environment and the
denatured protein can then act as a nucleating agent which is
deposited on and stains or discolors tooth enamel.
Previously employed additives which reduced dental staining by
cationic antibacterial antiplaque agents also generally reduced the
activity of antibacterial antiplaque agents such as bis-biguanido
compounds, as by forming a precipitate with such agents.
It is an advantage of this invention that anti-nucleating
additives, e.g. 2-phosphono butane-tricarboxylic acid (PBTA) and
its salts, are provided which unexpectedly inhibit, i.e. prevent or
remove, the staining of dental enamel caused by such cationic or
long chain tertiary amine antibacterial agents without
precipitating or substantially adversely affecting their
antibacterial and antiplaque activity. In themselves (even in the
absence of such antibacterial agents), these additives are
effective to reduce formation of dental calculus without unduly
decalcifying dental enamel, as disclosed and claimed in our
concurrently filed application Ser. No. 69,463 I.R. 3,651 entitled
Anticalculus Oral Composition, in addition to effectively
inhibiting gingivitis. However, not all anti-nucleating agents are
effective to prevent staining by such antibacterial agents.
Victamide (also known as Victamine C) which is a condensation
product of ammonia with phosphoruspentoxide, actually increases
staining even in the absence of such antibacterial agents.
In accordance with certain of its aspects, this invention relates
to an oral composition comprising an oral (orally acceptable)
vehicle, at least one cationic or long chain tertiary amine
antibacterial antiplaque agent which causes staining, and, as
antistaining additive, an effective stain-inhibiting amount of a
2-phosphono-butane-1,2,4-tricarboxylic acid (PBTA) compound, of the
formula ##STR3## wherein R is hydrogen, lower alkyl or carboxyl,
and R.sup.1 is hydrogen or methyl, or an orally acceptable salt
thereof, preferably water soluble, such as with an alkali metal
(e.g. sodium and potassium), ammonium, C.sub.1 -C.sub.18 mono-, di-
and tri-substituted ammonium (e.g. alkanol substituted such as
mono-, di- and tri-ethanolammonium) cation.
Compounds of the above formula, and methods for their production,
are disclosed in U.S. Pat. Nos. 3,886,204 and 3,886,205, which
disclosures are incorporated herein by reference thereto. The
preferred PBTA compound for use in the present invention is the
unsubstituted compound of the above formula (I) in which R and
R.sup.1 are each hydrogen. When R is lower alkyl, it preferably
contains 1 to 4 carbon atoms, especially methyl.
The concentration of these additives in oral compositions can range
widely, typically upward from about 0.01% by weight with no upper
limit except as dictated by cost or incompatibility with the
vehicle. Generally, concentrations of about 0.01% to about 10% and
preferably about 0.1% to 6% by weight are utilized. Oral
compositions which in the ordinary course of usage could be
accidentally ingested preferably contain lower concentrations of
these additives. Thus, a mouthwash in accordance with this
invention preferably contains less than about 2 weight % of the
additive, preferably about 0.1-1.5 wt%. Dentifrice compositions,
topical solutions and prophylactic pastes, the latter to be
administered professionally, can preferably contain about 0.1 to 3
weight % of the additive. Most desirably the additive is present in
a molar excess relative to the amount of antibacterial antiplaque
agent (based on its free base form) in order to best minimize,
inhibit or prevent staining.
Nitrogen-containing antibacterial agents which are cationic or long
chain amine germicides which may be employed in the practice of
this invention are described above. They are typically employed in
amounts such that the oral product contains between about 0.001 and
15% by weight of the agent. Preferably for desired levels of
antiplaque effect, the finished oral product contains about 0.01 to
about 5%, and most preferably about 0.25 to 1.0% by weight of the
antibacterial agent, referring to its free base form.
In certain highly preferred forms of the invention, the oral
composition may be substantially liquid in character, such as a
mouthwash or rinse. In such a preparation the vehicle is typically
a water-alcohol mixture. Generally, the ratio of water to alcohol
is in the range of from about 1:1 to about 20:1 preferably from 3:1
to 20:1 and most preferably about 17:3, by weight. The total amount
of water-alcohol mixture in this type of preparation is typically
in the range of from about 70 to about 99.9% by weight of the
preparation. The pH of such liquid and other preparations of the
invention is generally in the range of from about 4.5 to about 9
and typically from about 5.5 to 8. The pH is preferably in the
range of from about 6 to about 8.0. It is noteworthy that the
compositions of the invention may be applied orally at a pH below 5
without substantially decalcifying dental enamel.
Such liquid oral preparations may also contain a surface active
agent and/or a fluorine-providing compound.
In certain other desirable forms of this invention, the oral
composition may be substantially solid or pasty in character, such
as toothpowder, a dental tablet, a toothpaste or dental cream. The
vehicle of such solid or pasty oral preparations contains polishing
material. Examples of polishing materials are water-insoluble
sodium metaphosphate, potassium metaphosphate, tricalcium
phosphate, calcium pyrophosphate, magnesium orthophosphate,
trimagnesium phosphate, calcium carbonate, alumina, hydrated
alumina, aluminum silicate, zirconium silicates, bentonite, and
mixtures thereof. Preferred polishing materials include complex
amorphous alkali metal aluminosilicate and hydrated alumina.
Alumina, particularly the hydrated alumina sold by Alcoa as C333,
which has an alumina content of 64.9% by weight, a silica content
of 0.008%, a ferric oxide content of 0.003%, and a moisture content
of 0.37%, at 100.degree. C., and which has a specific gravity of
2.42 and a particle size such that 100% of the particles are less
than 50 microns and 84% of the particles are less than 20 microns,
is particularly desirable.
When visually clear gels are employed, polishing agents comprising
alkali metal aluminosilicate complexes are particularly useful,
since they have refractive indices close to the refractive indices
of gelling agent-liquid (including water and/or humectant) systems
commonly used in dentifrices.
Many of the so-called "water-soluble" polishing materials are
anionic in character and also include small amounts of soluble
material. Thus, insoluble sodium metaphosphate may be formed in any
suitable manner, as illustrated in Thorpe's Dictionary of Applied
Chemistry, Volume 9, Fourth Edition, pp. 510-511. The forms of
insoluble sodium metaphosphate known as Madrell's salt and Kunrol's
salt are further examples of suitable materials. These
metaphosphate salts exhibit a minute solubility in water, and
therefore are commonly referred to as insoluble metaphosphates.
There is present therein a minor amount of soluble phosphate
material as impurities, usually a few percent such as up to 4% by
weight. The amount of soluble phosphate material, which is believed
to include a soluble sodium trimetaphosphate in the case of
insoluble metaphosphate, may be reduced by washing with water if
desired. The insoluble alkali metal metaphosphate is typically
employed in powder form of a particle size such that no more than
about 1% of the material is larger than 37 microns.
The polishing material is generally present in amounts ranging from
about 10 to about 99% by weight of the oral preparation.
Preferably, it is present in amounts ranging from about 10 to about
75% in toothpaste, and from about 70 to about 99% in
toothpowder.
In the preparation of toothpowders, it is usually sufficient to
admix mechanically, e.g., by milling, the various solid ingredients
in appropriate quantities and particle sizes.
In pasty oral preparations the above-defined combination of the
antibacterial antiplaque agent and additive should be compatible
with the other components of the preparation. Thus, in a
toothpaste, the liquid vehicle may comprise water and humectant
typically in an amount ranging from about 10 to about 90% by weight
of the preparation. Glycerine, sorbitol, or polyethylene glycol may
also be present as humectants or binders. Particularly advantageous
liquid ingredients are polyethylene glycol and polypropylene
glycol. Also advantageous are liquid mixtures of water, glycerine
and sorbitol.
In clear gels where the refractive index is an important
consideration, about 3-30% by weight of water, 0 to about 80% by
weight of glycerine, and about 20-80% by weight of sorbitol is
preferably employed. A gelling agent, such as natural or synthetic
gums or gumlike materials, typically Irish moss, sodium
carboxymethylcellulose, methyl cellulose, hydroxyethyl cellulose,
gum tragacanth, polyvinylpyrrolidone, starch, or preferably
hydroxypropyl methyl cellulose or the Carbopols (e.g. 934,940 and
941) or the like is usually present in toothpaste in an amount up
to about 10% by weight, preferably in the range of from about 0.5
to about 5%. In a toothpaste or gel, the liquids and solids are
proportioned to form a creamy or gelled mass which is extrudable
from a pressurized container or from a collapsible, e.g., aluminum
or lead, tube.
The solid or pasty oral preparation which typically has a pH
measured on a 20% slurry of about 4.5 to 9, generally about 5.5 to
about 8 and preferably about 6 to about 8.0 may also contain a
surface active agent and/or a fluorine-providing compound.
It will be understood that, as is conventional, the oral
preparations are to be sold or otherwise distributed in suitable
labelled packages. Thus a jar of mouthrinse will have a label
describing it, in substance, as a mouthrinse or mouthwash and
having directions for its use; and a toothpaste will usually be in
a collapsible tube, typically aluminum or lined lead, or other
squeeze dispenser for metering out the contents, having a label
describing it, in substance, as a toothpaste or dental cream.
In oral compositions such as mouthrinses and toothpastes, a
surfactant is often present, e.g. to promote foaming. It will be
understood that it is preferable to employ nonionic surfactants
rather than their anionic counterparts. Examples of water-soluble
nonionic surfactants are condensation products of ethylene oxide
with various reactive hydrogen-containing compounds reactive
therewith having long hydrophobic chains (e.g. aliphatic chains of
about 12 to 20 carbon atoms), which condensation products
("ethoxamers") contain hydrophilic polyoxyethylene moieties, such
as condensation products of ethylene oxide with fatty acids, fatty
alcohols and fatty amides including alcohols such as sorbitan
monostearate or polypropyleneoxide (that is Pluronic
materials).
In certain forms of this invention a fluorine-providing compound is
present in the oral preparation. These compounds may be slightly
soluble in water or may be fully water-soluble. They are
characterized by their ability to release fluoride ions in water
and by substantial freedom from reaction with other compounds of
the oral preparation. Among these materials are inorganic fluoride
salts, such as soluble alkali metal, alkaline earth metal and heavy
metal salts, for example, sodium fluoride, potassium fluoride,
ammonium fluoride, a copper fluoride such as cuprous fluoride, zinc
fluoride, a tin fluoride such as stannic fluoride or stannous
chlorofluoride, barium fluoride, sodium fluorsilicate, ammonium
fluorosilicate, sodium fluorozirconate, sodium monofluorophosphate,
aluminum mono- and di-fluorophosphate, and fluorinated sodium
calcium pyrophosphate. Alkali metal and tin fluorides, such as
sodium and stannous fluorides, sodium monofluorophosphate and
mixtures therof, are preferred.
The amount of the fluorine-providing compound is dependent to some
extent upon the type of compound, its solubility, and the type or
oral preparation, but it must be a nontoxic amount. In a solid oral
preparation, such as toothpaste or toothpowder, an amount of such
compound which releases a maximum of about 1% by weight of the
preparation is considered satisfactory. Any suitable minimum amount
of such compound may be used, but it is preferable to employ
sufficient compound to release about 0.005 to 1%, and preferably
about 0.1% of fluoride ion. Typically, in the cases of alkali metal
fluorides and stannous fluoride, this component is present in an
amount up to about 2% by weight, based on the weight of the
preparation, and preferably in the range of about 0.05 to 1%. In
the case of sodium monofluorophosphate, the compound may be present
in an amount up to 7.6% by weight, more typically about 0.76%.
In a liquid oral preparation such as a mouthwash, the
fluorine-providing compound is typically present in an amount
sufficient to release up to about 0.13%, preferably about 0.0013 to
0.1% and most preferably about 0.0013 to 0.05%, by weight, of
fluoride ion.
Various other materials may be incorporated in the oral
preparations of this invention. Examples are whitening agents,
preservatives, silicones, chlorophyll compounds, and ammoniated
material such as urea, diammonium phosphate, and mixtures thereof.
These adjuvants, where present, are incorporated in the
preparations in amounts which do not substantially adversely affect
the properties and characteristics desired.
Any suitable flavoring or sweetening material may also be employed.
Examples of suitable flavoring constituents are flavoring oils,
e.g., oils of spearmint, peppermint, wintergreen, sassafras, clove,
sage, eucalyptus, marjoram, cinnamon, lemon and orange, and methyl
salicylate. Suitable sweetening agents include sucrose, lactose,
maltose, sorbitol, sodium cyclamate, perillartine, APM*,
saccharine. Suitably, flavor and sweetening agents may together
comprise from about 0.1 to 5% or more of the preparation.
In preparing the oral compositions of this invention comprising the
above-defined combination of antibacterial agent and additive in an
oral vehicle which typically includes water, it is highly preferred
if not essential to add the additive after the other ingredients
(except perhaps some of the water) are mixed or contacted with each
other to avoid a tendency for said agent to be precipitated.
For instance, a mouthrinse or mouthwash may be prepared by mixing
ethanol and water with flavoring oil, nonionic surfactant,
humectant, cationic antibacterial antiplaque agent, such as
benzethonium chloride or chlorohexidine, sweetener, color and then
the above-defined additive, followed by additional water as
desired.
A toothpaste may be prepared by forming a gel with humectant, gum
or thickener such as hydroxyethyl cellulose, sweetener and adding
thereto polishing agent, flavor, antibacterial agent, such as
benzethonium chloride or chlorhexidine, additional water, and then
the above-defined additive. If sodium carboxymethyl cellulose is
employed as the gelling agent, the procedure of either U.S. Pat.
No. 3,842,168 or U.S. Pat. No. 3,843,779, modified by the inclusion
of the additive, is followed.
In the practice of this invention an oral composition according to
this invention such as a mouthwash or toothpaste containing
cationic or long chain amine antibacterial antiplaque agent in an
amount effective to promote oral hygiene and the defined additive
in an amount effective to reduce staining of dental surfaces
otherwise resulting from the presence of the antibacterial
antiplaque agent, is applied regularly to dental enamel, preferably
from about 5 times per week to about 3 times daily, at a pH of
about 4.5 to about 9, generally about 5.5 to about 8, preferably
about 6 to 8.
The following specific examples are further illustrative of the
nature of the present invention, but it is understood that the
invention is not limited thereto. All amounts and proportions
referred to herein and the appended claims are by weight unless
otherwise indicated.
Table I below is illustrative of mouthwash formulations according
to the invention and the antistaining activity of the preferred
PBTA additive therein. The tooth staining characteristics of the
formulations are evaluated by slurrying hydroxyapatite (Biogel), a
specific salivary protein, a carbonyl source (e.g. acetaldehyde),
and a pH 7 phosphate buffer, with and without the mouthwash
formulations being tested. The mixture is shaken at 37.degree. C.
for 18 hours. The colored HAP powder is separated by filtration,
dried and the color levels (in reflectance units) determined on a
Gardner color difference meter.
TABLE I
__________________________________________________________________________
CLEAR MOUTHWASH FORMULATIONS Example (1) (2) (3) (4) (5) (6) (7)
__________________________________________________________________________
Ethanol 10% 10% 10% 10% 10% 10% 10% Glycerine 10 10 10 10 10 10 10
Pluronic F108.sup.1 3.0 3.0 3.0 3.0 3.0 3.0 3.0 Flavor 0.146 0.146
0.146 0.146 0.146 0.146 0.146 Saccharin (Na) 0.03 0.03 0.03 0.03
0.03 0.03 0.03 CPC.sup.2 0.1 0.1 0.1 0.1 0.1 0.1 PBTA 0.1 0.2 0.3
0.5 1.0 Water, g.s. to 100% 100% 100% 100% 100% 100% 100% pH (with
1N NaOH) 7.0 7.0 7.0 7.0 7.0 7.0 7.0 Reflectance 56.8 39.6 42.1
43.6 46.2 47.8 55.9 Difference -- +17.2 -2.5 -4.0 -6.6 -8.2 -16.3
RD .vertline..rarw. COMPARED TO EXAMPLE (2) .fwdarw. .vertline.
__________________________________________________________________________
.sup.1 Polyalkyle .sup.2 Cetyl pyridinium chloride.
The above results plainly establish that the additives of the
present invention, as exemplified by PBTA, substantially reduce
dental staining ordinarily produced by cationic quaternary ammonia
antibacterial antiplaque agents as exemplified by CPC. A PBTA
concentration of about 1.0% appears to yield excellent results.
Such additives also reduce or inhibit gingivitis and do not
significantly reduce the antiplaque activity of the indicated
antiplaque agents.
Substitution of equivalent amounts of the following anti-bacterial
antiplaque agents for the CPC employed in Examples 3-7 yield
formulations also producing an unexpected reduction in dental
staining.
______________________________________ Example Antibacterial
Antiplaque Agent ______________________________________ 8
benzethonium chloride (BC) 9 chlorhexidine diacetate 10
chlorohexidine digluconate 11 dodecyl trimethyl ammonium bromide 12
cetyl pyridinium chloride 13 ##STR4## 14 alexidine dihydrochloride
______________________________________
The following formulations exemplify toothpastes with antiplaque
activity and reduced staining.
______________________________________ Example (Parts) 18 19 20
______________________________________ Hydrated alumina 30 30 30
Polyethylene glycol 600 22 22 22 Pluronic F-108 3 3 3 Hydroxypropyl
methyl cellulose 1.2 1.2 1.2 BC 0.5 -- -- Hibitane -- 4.725 -- CPC
-- -- 0.5 PBTA 1.0 1.0 1.0 Sodium saccharin 0.17 0.17 0.17 Flavor
0.8 0.8 0.8 Water g.s to 100 100 100
______________________________________
Significant reductions in dental staining plaque and gingivitis are
also obtained according to the present invention when the PBTA in
the above example is replaced by any of the other PBTA compounds
disclosed in U.S. Pat. Nos. 3,886,204 and 3,886,205.
This invention has been described with respect to preferred
embodiments and it will be understood that modifications and
variations thereof obvious to those skilled in the art are to be
included within the spirit and purview of this application and the
scope of the appended claims.
* * * * *